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Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair

OBJECTIVE: Esophageal adenocarcinoma (EAC) continues to be a disease associated with high mortality. Among the factors leading to poor outcomes are innate resistance to currently available therapies, advanced stage at diagnosis, and complex biology. Platinum and ionizing radiation form the backbone...

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Autores principales: Dewalt, Robin I, Kesler, Kenneth A, Hammoud, Zane T, Baldridge, LeeAnn, Hattab, Eyas M, Jalal, Shadia I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217507/
https://www.ncbi.nlm.nih.gov/pubmed/28210138
http://dx.doi.org/10.2147/LCTT.S57594
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author Dewalt, Robin I
Kesler, Kenneth A
Hammoud, Zane T
Baldridge, LeeAnn
Hattab, Eyas M
Jalal, Shadia I
author_facet Dewalt, Robin I
Kesler, Kenneth A
Hammoud, Zane T
Baldridge, LeeAnn
Hattab, Eyas M
Jalal, Shadia I
author_sort Dewalt, Robin I
collection PubMed
description OBJECTIVE: Esophageal adenocarcinoma (EAC) continues to be a disease associated with high mortality. Among the factors leading to poor outcomes are innate resistance to currently available therapies, advanced stage at diagnosis, and complex biology. Platinum and ionizing radiation form the backbone of treatment for the majority of patients with EAC. Of the multiple processes involved in response to platinum chemotherapy or ionizing radiation, deoxyribonucleic acid (DNA) repair has been a major player in cancer sensitivity to these agents. DNA repair defects have been described in various malignancies. The purpose of this study was to determine whether alterations in DNA repair are present in EAC compared with normal gastroesophageal tissues. METHODS: We analyzed the expression of genes involved in homologous recombination (HR), nonhomologous end-joining, and nucleotide excision repair (NER) pathways in 12 EAC tumor samples with their matched normal counterparts. These pathways were chosen because they are the main pathways involved in the repair of platinum- or ionizing-radiation-induced damage. In addition, abnormalities in these pathways have not been well characterized in EAC. RESULTS: We identified increased expression of at least one HR gene in eight of the EAC tumor samples. Alterations in the expression of EME1, a structure-specific endonuclease involved in HR, were the most prevalent, with messenger (m)RNA overexpression in six of the EAC samples. In addition, all EAC samples revealed decreased expression of at least one of numerous NER genes including XPC, XPA, DDB2, XPF, and XPG. CONCLUSION: Our study identified DNA repair dysregulation in EAC involving two critical pathways, HR and NER, and is the first demonstration of EME1 upregulation in any cancer. These DNA repair abnormalities have the potential to affect a number of processes such as genomic instability and therapy response, and the consequences of these defects deserve further study in EAC.
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spelling pubmed-52175072017-02-16 Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair Dewalt, Robin I Kesler, Kenneth A Hammoud, Zane T Baldridge, LeeAnn Hattab, Eyas M Jalal, Shadia I Lung Cancer (Auckl) Original Research OBJECTIVE: Esophageal adenocarcinoma (EAC) continues to be a disease associated with high mortality. Among the factors leading to poor outcomes are innate resistance to currently available therapies, advanced stage at diagnosis, and complex biology. Platinum and ionizing radiation form the backbone of treatment for the majority of patients with EAC. Of the multiple processes involved in response to platinum chemotherapy or ionizing radiation, deoxyribonucleic acid (DNA) repair has been a major player in cancer sensitivity to these agents. DNA repair defects have been described in various malignancies. The purpose of this study was to determine whether alterations in DNA repair are present in EAC compared with normal gastroesophageal tissues. METHODS: We analyzed the expression of genes involved in homologous recombination (HR), nonhomologous end-joining, and nucleotide excision repair (NER) pathways in 12 EAC tumor samples with their matched normal counterparts. These pathways were chosen because they are the main pathways involved in the repair of platinum- or ionizing-radiation-induced damage. In addition, abnormalities in these pathways have not been well characterized in EAC. RESULTS: We identified increased expression of at least one HR gene in eight of the EAC tumor samples. Alterations in the expression of EME1, a structure-specific endonuclease involved in HR, were the most prevalent, with messenger (m)RNA overexpression in six of the EAC samples. In addition, all EAC samples revealed decreased expression of at least one of numerous NER genes including XPC, XPA, DDB2, XPF, and XPG. CONCLUSION: Our study identified DNA repair dysregulation in EAC involving two critical pathways, HR and NER, and is the first demonstration of EME1 upregulation in any cancer. These DNA repair abnormalities have the potential to affect a number of processes such as genomic instability and therapy response, and the consequences of these defects deserve further study in EAC. Dove Medical Press 2014-02-15 /pmc/articles/PMC5217507/ /pubmed/28210138 http://dx.doi.org/10.2147/LCTT.S57594 Text en © 2014 Dewalt et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Dewalt, Robin I
Kesler, Kenneth A
Hammoud, Zane T
Baldridge, LeeAnn
Hattab, Eyas M
Jalal, Shadia I
Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
title Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
title_full Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
title_fullStr Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
title_full_unstemmed Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
title_short Gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
title_sort gastroesophageal junction adenocarcinoma displays abnormalities in homologous recombination and nucleotide excision repair
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217507/
https://www.ncbi.nlm.nih.gov/pubmed/28210138
http://dx.doi.org/10.2147/LCTT.S57594
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